Cui Jiajia, Liu Yuetao, Hu Yinghuan, Tong Jiayu, Li Aiping, Qu Tingli, Qin Xuemei, Du Guanhua
Modern Research Center for Traditional Chinese Medicine of Shanxi University, No. 92, Wucheng Road, Taiyuan 030006, Shanxi, PR China.
Modern Research Center for Traditional Chinese Medicine of Shanxi University, No. 92, Wucheng Road, Taiyuan 030006, Shanxi, PR China.
J Pharm Biomed Anal. 2017 Jan 5;132:77-86. doi: 10.1016/j.jpba.2016.09.044. Epub 2016 Sep 28.
Chronic atrophic gastritis (CAG) is one of the most important pre-cancerous states with a high prevalence. Exploring of the underlying mechanism and potential biomarkers is of significant importance for CAG. In the present work, H NMR-based metabonomics with correlative analysis was performed to analyze the metabolic features of CAG. 19 plasma metabolites and 18 urine metabolites were enrolled to construct the circulatory and excretory metabolome of CAG, which was in response to alterations of energy metabolism, inflammation, immune dysfunction, as well as oxidative stress. 7 plasma biomarkers and 7 urine biomarkers were screened to elucidate the pathogenesis of CAG based on the further correlation analysis with biochemical indexes. Finally, 3 plasma biomarkers (arginine, succinate and 3-hydroxybutyrate) and 2 urine biomarkers (α-ketoglutarate and valine) highlighted the potential to indicate risks of CAG in virtue of correlation with pepsin activity and ROC analysis. Here, our results paved a way for elucidating the underlying mechanisms in the development of CAG, and provided new avenues for the diagnosis of CAG and presented potential drug targets for treatment of CAG.
慢性萎缩性胃炎(CAG)是最重要的癌前状态之一,患病率很高。探索其潜在机制和潜在生物标志物对CAG具有重要意义。在本研究中,采用基于核磁共振氢谱的代谢组学结合相关分析来分析CAG的代谢特征。纳入19种血浆代谢物和18种尿液代谢物以构建CAG的循环和排泄代谢组,这与能量代谢、炎症、免疫功能障碍以及氧化应激的改变有关。基于与生化指标的进一步相关分析,筛选出7种血浆生物标志物和7种尿液生物标志物以阐明CAG的发病机制。最后,3种血浆生物标志物(精氨酸、琥珀酸和3-羟基丁酸)和2种尿液生物标志物(α-酮戊二酸和缬氨酸)通过与胃蛋白酶活性的相关性及ROC分析,显示出指示CAG风险的潜力。在此,我们的结果为阐明CAG发生发展的潜在机制铺平了道路,为CAG的诊断提供了新途径,并为CAG的治疗提供了潜在的药物靶点。